Velvet Ice Cream Recalls Cookies n Cream Tub for Listeria Risk
Velvet Ice Cream Company is recalling Whale of Pail Cookies n Cream gallon tubs due to potential Listeria monocytogenes contamination.
The agency’s classification
FDA (Food): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class I, which indicates a reasonable probability that the use of, or exposure to, the violative product will cause serious adverse health consequences or death. The rubric mandates a score of at least 4 for FDA Class I recalls.
Plain-English summary
Velvet Ice Cream Company is voluntarily recalling Whale of Pail Cookies n Cream Gallon Plastic Tub ice cream. The recall is being issued because the product is potentially contaminated with Listeria monocytogenes.
The affected product is identified by Lot 21090. It was distributed in Illinois, Indiana, Kentucky, Michigan, Ohio, South Carolina, West Virginia, Pennsylvania, and New York.
Consumers who have purchased this product should stop using it and dispose of it or return it to the place of purchase.
The recalled product
- Product
- Whale of Pail Cookies n Cream Gallon Plastic Tub
- Manufacturer
- Velvet Ice Cream Company
- Category
- Food — Ice Cream
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot 21090
Distribution
Part of a larger recall action
This product is one of 56 recalled by Velvet Ice Cream Company under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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